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Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis

BACKGROUND: The aim was to determine the level of inflammatory cytokines, eosinophil cationic protein and IgE in allergic rhinitis (AR) patients. SUBJECTS AND METHODS: Blood samples were taken from 88 AR patients and 88 healthy controls (HC). Each sample was analysed for eosinophil counts by flow cy...

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Autores principales: Amin, Kawa, Issa, Sulaf Mosa, Ali, Kosar Mohammad, Aziz, Muaid Ismiel, Hama Amieen, Huner Mohamed, Bystrom, Jonas, Janson, Christer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129325/
https://www.ncbi.nlm.nih.gov/pubmed/32280308
http://dx.doi.org/10.1186/s12948-020-00117-6
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author Amin, Kawa
Issa, Sulaf Mosa
Ali, Kosar Mohammad
Aziz, Muaid Ismiel
Hama Amieen, Huner Mohamed
Bystrom, Jonas
Janson, Christer
author_facet Amin, Kawa
Issa, Sulaf Mosa
Ali, Kosar Mohammad
Aziz, Muaid Ismiel
Hama Amieen, Huner Mohamed
Bystrom, Jonas
Janson, Christer
author_sort Amin, Kawa
collection PubMed
description BACKGROUND: The aim was to determine the level of inflammatory cytokines, eosinophil cationic protein and IgE in allergic rhinitis (AR) patients. SUBJECTS AND METHODS: Blood samples were taken from 88 AR patients and 88 healthy controls (HC). Each sample was analysed for eosinophil counts by flow cytometry, IgE by ECLIA, ECP, IL-17, and IL-33 by using ELISA test. RESULTS: There was no significant difference between AR patients and the control group in age and gender. Levels of eosinophils, IgE, ECP, IL-17, IL-33 and the total symptom scores were significantly higher in AR patients than the HC (P = 0.0001). Serum ECP correlated with IL-17 (P = 0.041, r = 0.42), IL-33 (P = 0.0001, r = 080), and IgE levels (P = 0.017, r = 0.45) in the R patients. There was no correlation between IL-17 and IL-33. There was a correlation between symptom scores and eosinophils (P = 0.026, r = 0.52), and IgE (P = 0.001, r = 0.60) in the patients. No correlation was observed between symptom scores and ECP, IL-17, and IL-33 in the AR patient. CONCLUSIONS: Patients with AR have significant higher serum levels of ECP, IL-17, and IL-33 than healthy controls. This indicates that these markers could be used to in order to diagnose AR and to monitor disease. Inhibitory molecules to IL-17 and IL-33 may be considered as novel treatment strategies.
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spelling pubmed-71293252020-04-10 Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis Amin, Kawa Issa, Sulaf Mosa Ali, Kosar Mohammad Aziz, Muaid Ismiel Hama Amieen, Huner Mohamed Bystrom, Jonas Janson, Christer Clin Mol Allergy Research BACKGROUND: The aim was to determine the level of inflammatory cytokines, eosinophil cationic protein and IgE in allergic rhinitis (AR) patients. SUBJECTS AND METHODS: Blood samples were taken from 88 AR patients and 88 healthy controls (HC). Each sample was analysed for eosinophil counts by flow cytometry, IgE by ECLIA, ECP, IL-17, and IL-33 by using ELISA test. RESULTS: There was no significant difference between AR patients and the control group in age and gender. Levels of eosinophils, IgE, ECP, IL-17, IL-33 and the total symptom scores were significantly higher in AR patients than the HC (P = 0.0001). Serum ECP correlated with IL-17 (P = 0.041, r = 0.42), IL-33 (P = 0.0001, r = 080), and IgE levels (P = 0.017, r = 0.45) in the R patients. There was no correlation between IL-17 and IL-33. There was a correlation between symptom scores and eosinophils (P = 0.026, r = 0.52), and IgE (P = 0.001, r = 0.60) in the patients. No correlation was observed between symptom scores and ECP, IL-17, and IL-33 in the AR patient. CONCLUSIONS: Patients with AR have significant higher serum levels of ECP, IL-17, and IL-33 than healthy controls. This indicates that these markers could be used to in order to diagnose AR and to monitor disease. Inhibitory molecules to IL-17 and IL-33 may be considered as novel treatment strategies. BioMed Central 2020-04-04 /pmc/articles/PMC7129325/ /pubmed/32280308 http://dx.doi.org/10.1186/s12948-020-00117-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Amin, Kawa
Issa, Sulaf Mosa
Ali, Kosar Mohammad
Aziz, Muaid Ismiel
Hama Amieen, Huner Mohamed
Bystrom, Jonas
Janson, Christer
Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis
title Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis
title_full Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis
title_fullStr Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis
title_full_unstemmed Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis
title_short Evidence for eosinophil and IL-17 mediated inflammation in allergic rhinitis
title_sort evidence for eosinophil and il-17 mediated inflammation in allergic rhinitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129325/
https://www.ncbi.nlm.nih.gov/pubmed/32280308
http://dx.doi.org/10.1186/s12948-020-00117-6
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